Morphological and mechanical examination of the atrial 'intima'.

AIMS To examine morphology and mechanical properties of the atrial 'intima', which we defined as the tissue interposed between atrial endocardium and myocardium, in patients without known cardiovascular disease. METHODS AND RESULTS Post-mortem right and left atrial tissue was obtained from male infants (<1 year, n = 4), children (10-19 years, n = 4), and adults (58-69 years, n = 7). Using light microscopy and an ocular micrometer, atrial intimal (AIT) thickness was measured. Intimal collagen bundle thickness was measured using electron microscopy. Passive atrial wall stiffness was measured using a planar biaxial testing device. Among infants, left AIT (0.2 ± 0.2 mm) and right (0.2 ± 0.1 mm) AIT were not significantly different (P = 0.84). Among children, left AIT (0.6 ± 0.2 mm) was significantly greater than right (0.2 ± 0.1 mm) AIT (P = 0.03), and left AIT was marginally greater than in infants (P = 0.07). Among adults, with the exception of the appendage region, left AIT (1.0 ± 0.2 mm) was markedly greater than right AIT (0.3 ± 0.1 mm; P < 0.05), and left AIT was significantly greater than that in other age groups (P < 0.05). There were no differences in right AIT among age groups. Left intimal collagen bundle thickness was greater in adults (0.0512 ± 0.0056 µm) than infants (0.0432 ± 0.0071 µm) or children (0.0435 ± 0.0013 µm), and bundles were less organized. Wall stiffness was attributable primarily to the intima (1245 ± 132, vs. 260 ± 45 N/m(2) for the remaining atrial wall). CONCLUSION The left atrial intima, but not the right, thickens with age, becomes more disorganized ultrastructurally, and is responsible for the majority of atrial wall stiffness.

[1]  Yiling Lu,et al.  Left Atrial Wall Stress Distribution and Its Relationship to Electrophysiologic Remodeling in Persistent Atrial Fibrillation , 2012, Circulation. Arrhythmia and electrophysiology.

[2]  C. Ayers,et al.  Left atrial structure and function and clinical outcomes in the general population. , 2013, European heart journal.

[3]  H. Tsao,et al.  Aging dilates atrium and pulmonary veins: implications for the genesis of atrial fibrillation. , 2008, Chest.

[4]  Angel López‐Candales,et al.  The Importance of Increased Interatrial Septal Thickness in Patients with Atrial Fibrillation: A Transesophageal Echocardiographic Study , 2005, Echocardiography.

[5]  Julio E. Pérez,et al.  Effects of aging on left atrial reservoir, conduit, and booster pump function: a multi-institution acoustic quantification study , 2001, Heart.

[6]  D H Blankenhorn,et al.  A definition of the intima of human arteries and of its atherosclerosis-prone regions. A report from the Committee on Vascular Lesions of the Council on Arteriosclerosis, American Heart Association. , 1992, Circulation.

[7]  Kevin J. Parker,et al.  Techniques for elastic imaging: a review , 1996 .

[8]  R. Lannigan,et al.  Ultrastructure of the normal atrial endocardium. , 1966, British heart journal.

[9]  M. Schalij,et al.  Histology of vascular myocardial wall of left atrial body after pulmonary venous incorporation. , 2006, The American journal of cardiology.

[10]  Chiara Bellini,et al.  In vivo porcine left atrial wall stress: Effect of ventricular tachypacing on spatial and temporal stress distribution. , 2011, Journal of biomechanics.

[11]  M. Sacks Biaxial Mechanical Evaluation of Planar Biological Materials , 2000 .

[12]  E. Lakatta Age-associated Cardiovascular Changes in Health: Impact on Cardiovascular Disease in Older Persons , 2004, Heart Failure Reviews.

[13]  Chiara Bellini,et al.  In vivo porcine left atrial wall stress: Computational model. , 2011, Journal of biomechanics.

[14]  E. Lakatta,et al.  Arterial Aging: A Journey Into Subclinical Arterial Disease , 2010, Current opinion in nephrology and hypertension.